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1025909-06-1

(1E,3Z)-11-Methoxymethoxy-1-(4-methoxy-phenyl)-4-methyl-undeca-1,3-dien-8-yn-5-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1025909-06-1 Structure

  • Basic information

    1. Product Name: (1E,3Z)-11-Methoxymethoxy-1-(4-methoxy-phenyl)-4-methyl-undeca-1,3-dien-8-yn-5-ol
    2. Synonyms:
    3. CAS NO:1025909-06-1
    4. Molecular Formula:
    5. Molecular Weight: 344.451
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1025909-06-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1E,3Z)-11-Methoxymethoxy-1-(4-methoxy-phenyl)-4-methyl-undeca-1,3-dien-8-yn-5-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1E,3Z)-11-Methoxymethoxy-1-(4-methoxy-phenyl)-4-methyl-undeca-1,3-dien-8-yn-5-ol(1025909-06-1)
    11. EPA Substance Registry System: (1E,3Z)-11-Methoxymethoxy-1-(4-methoxy-phenyl)-4-methyl-undeca-1,3-dien-8-yn-5-ol(1025909-06-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1025909-06-1(Hazardous Substances Data)

1025909-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025909-06-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,9,0 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1025909-06:
(9*1)+(8*0)+(7*2)+(6*5)+(5*9)+(4*0)+(3*9)+(2*0)+(1*6)=131
131 % 10 = 1
So 1025909-06-1 is a valid CAS Registry Number.

1025909-06-1Relevant articles and documents

Transition metal-catalyzed intramolecular [4+2] cycloadditions: Mechanistic and synthetic investigations

Wender, Paul A.,Smith, Thomas E.

, p. 1255 - 1275 (1998)

The nickel-catalyzed intramolecular cycloaddition of dienes with unactivatable alkynes is found to proceed under mild conditions while the corresponding Diels-Alder cycloaddition of the same substrates either fails of occurs only under forcing conditions. The nickel-catalyzed cycloaddition is also shown to occur with retention of stereochemistry and is not significantly influenced by electronic effects. Finally, the catalyzed process is shown to be applicable to the synthesis of angularly substituted bicycles, including the CD ring systems of steroids and vitamin D.

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